PT3766885T - Tricyclic compounds and their use as phosphodiesterase inhibitors - Google Patents
Tricyclic compounds and their use as phosphodiesterase inhibitorsInfo
- Publication number
- PT3766885T PT3766885T PT201931250T PT20193125T PT3766885T PT 3766885 T PT3766885 T PT 3766885T PT 201931250 T PT201931250 T PT 201931250T PT 20193125 T PT20193125 T PT 20193125T PT 3766885 T PT3766885 T PT 3766885T
- Authority
- PT
- Portugal
- Prior art keywords
- phosphodiesterase inhibitors
- tricyclic compounds
- tricyclic
- compounds
- phosphodiesterase
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
- C07D471/14—Ortho-condensed systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/506—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim not condensed and containing further heterocyclic rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/14—Decongestants or antiallergics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/22—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/12—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains three hetero rings
- C07D487/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/12—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains three hetero rings
- C07D491/14—Ortho-condensed systems
- C07D491/147—Ortho-condensed systems the condensed system containing one ring with oxygen as ring hetero atom and two rings with nitrogen as ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/22—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D513/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
- C07D513/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains three hetero rings
- C07D513/14—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D519/00—Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US201562180815P | 2015-06-17 | 2015-06-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
PT3766885T true PT3766885T (en) | 2022-08-09 |
Family
ID=56418558
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT167395631T PT3310784T (en) | 2015-06-17 | 2016-06-09 | Tricyclic compounds and their use as phosphodiesterase inhibitors |
PT201931250T PT3766885T (en) | 2015-06-17 | 2016-06-09 | Tricyclic compounds and their use as phosphodiesterase inhibitors |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PT167395631T PT3310784T (en) | 2015-06-17 | 2016-06-09 | Tricyclic compounds and their use as phosphodiesterase inhibitors |
Country Status (29)
Country | Link |
---|---|
US (3) | US11472805B2 (en) |
EP (2) | EP3766885B1 (en) |
JP (1) | JP6827959B2 (en) |
KR (2) | KR102426986B1 (en) |
CN (1) | CN107787322B (en) |
AU (2) | AU2016280137B2 (en) |
BR (1) | BR112017026191B1 (en) |
CA (1) | CA2989456C (en) |
CO (1) | CO2017012994A2 (en) |
CR (1) | CR20170572A (en) |
CU (1) | CU20170153A7 (en) |
DK (2) | DK3766885T3 (en) |
DO (1) | DOP2017000297A (en) |
EA (1) | EA039714B1 (en) |
EC (1) | ECSP18003372A (en) |
ES (2) | ES2832893T3 (en) |
HK (2) | HK1245790A1 (en) |
HU (2) | HUE051898T2 (en) |
IL (1) | IL255444B (en) |
MX (1) | MX2017016149A (en) |
PE (1) | PE20180478A1 (en) |
PH (1) | PH12017502260A1 (en) |
PL (2) | PL3310784T3 (en) |
PT (2) | PT3310784T (en) |
SG (1) | SG10201912333PA (en) |
TN (1) | TN2017000485A1 (en) |
TW (1) | TWI623538B (en) |
UA (1) | UA125334C2 (en) |
WO (1) | WO2016203347A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
HUE051898T2 (en) * | 2015-06-17 | 2021-03-29 | Pfizer | Tricyclic compounds and their use as phosphodiesterase inhibitors. |
CN109438448B (en) * | 2018-11-07 | 2021-08-27 | 成都大学 | Indolo-heptatomic ring compound and preparation method and application thereof |
JP2022518292A (en) * | 2019-01-23 | 2022-03-14 | パス セラピューティクス,インク. | Treatment of epilepsy by inhibition of phosphodiesterase 4 (PDE4) |
EP4188353A1 (en) * | 2020-07-26 | 2023-06-07 | Intra-Cellular Therapies, Inc. | Novel uses |
WO2023076547A1 (en) * | 2021-10-29 | 2023-05-04 | Sensorium Therapeutics, Inc. | Deuterated forms of alkaloid compounds and therapeutic uses thereof |
Family Cites Families (94)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3702321A (en) * | 1968-02-13 | 1972-11-07 | Sumitomo Chemical Co | Process for preparing benzodiazepine derivatives |
DE2005845A1 (en) | 1969-02-12 | 1970-09-03 | Sumitomo Chemical Company, Ltd., Osaka (Japan) | Process for the preparation of benzodiazepines and their salts |
CH560201A5 (en) | 1969-03-11 | 1975-03-27 | Hoffmann La Roche | 1 4-benzodiazepin derivs anti-convulsive, - muscle relaxant, tranquillising |
AT299964B (en) * | 1969-04-14 | 1972-07-10 | Sumitomo Chemical Co | Process for the preparation of new [2- (dioxo-piperazino) -benzoyl] -pyridine derivatives or salts thereof |
DE2144272A1 (en) * | 1971-09-03 | 1972-03-23 | Sumitomo Chemical Co Ltd , Osaka (Japan) | Nitro-benzodiazepines - prepn from 2-(2,3-diketopiperazino) nitrobenzophenones |
US4022778A (en) * | 1971-11-05 | 1977-05-10 | American Home Products Corporation | 10-Aryl-1,2,3,4-tetrahydropyrazino(1,2-α)indole and derivatives thereof |
JPS5033259B2 (en) * | 1972-03-31 | 1975-10-29 | ||
EP0028489B1 (en) | 1979-11-05 | 1983-10-05 | Beecham Group Plc | Enzyme derivatives, and their preparation |
EP0683234B2 (en) | 1993-01-25 | 2007-06-06 | Takeda Chemical Industries, Ltd. | Antibody against beta-amyloid or their derivative and use thereof |
US5612359A (en) | 1994-08-26 | 1997-03-18 | Bristol-Myers Squibb Company | Substituted biphenyl isoxazole sulfonamides |
TW536540B (en) | 1997-01-30 | 2003-06-11 | Bristol Myers Squibb Co | Endothelin antagonists: N-[[2'-[[(4,5-dimethyl-3-isoxazolyl)amino]sulfonyl]-4-(2-oxazolyl)[1,1'-biphenyl]-2-yl]methyl]-N,3,3-trimethylbutanamide and N-(4,5-dimethyl-3-isoxazolyl)-2'-[(3,3-dimethyl-2-oxo-1-pyrrolidinyl)methyl]-4'-(2-oxazolyl)[1,1'-biphe |
DE19709877A1 (en) | 1997-03-11 | 1998-09-17 | Bayer Ag | 1,5-dihydro-pyrazolo [3,4-d] pyrimidinone derivatives |
US8173127B2 (en) | 1997-04-09 | 2012-05-08 | Intellect Neurosciences, Inc. | Specific antibodies to amyloid beta peptide, pharmaceutical compositions and methods of use thereof |
NZ337765A (en) | 1997-04-09 | 2001-09-28 | Mindset Biopharmaceuticals Usa | Recombinant antibodies having specificity for beta-amyloid N-terminus and C-terminus and use in treating Alzheimer's Disease |
GB9722520D0 (en) | 1997-10-24 | 1997-12-24 | Pfizer Ltd | Compounds |
TWI239847B (en) | 1997-12-02 | 2005-09-21 | Elan Pharm Inc | N-terminal fragment of Abeta peptide and an adjuvant for preventing and treating amyloidogenic disease |
US6743427B1 (en) | 1997-12-02 | 2004-06-01 | Neuralab Limited | Prevention and treatment of amyloidogenic disease |
EP2002837A1 (en) | 1998-07-06 | 2008-12-17 | Bristol-Myers Squibb Company | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
IT1313593B1 (en) | 1999-08-03 | 2002-09-09 | Novuspharma Spa | 1,2-DIIDRO-1-OXO-PIRAZINO 1,2-A INDOL DERIVATIVES. |
MY125533A (en) | 1999-12-06 | 2006-08-30 | Bristol Myers Squibb Co | Heterocyclic dihydropyrimidine compounds |
AU4178601A (en) | 2000-02-24 | 2001-09-03 | Univ Washington | Humanized antibodies that sequester abeta peptide |
AU2001283955B2 (en) | 2000-07-31 | 2006-05-18 | F. Hoffmann-La Roche Ag | Piperazine derivatives |
DE10045112A1 (en) | 2000-09-11 | 2002-03-21 | Merck Patent Gmbh | Use of indole derivatives for the treatment of diseases of the central nervous system |
WO2002042429A2 (en) | 2000-11-03 | 2002-05-30 | Proteotech, Inc. | Methods of isolating amyloid-inhibiting compounds and use of compounds isolated from uncaria tomentosa and related plants |
EP1383501B1 (en) | 2001-02-28 | 2007-04-04 | Merck & Co., Inc. | Acylated piperidine derivatives as melanocortin-4 receptor agonists |
WO2002100350A2 (en) | 2001-06-13 | 2002-12-19 | The Regents Of University Of Michigan | Dopamine receptor ligands and therapeutic methods based thereon |
EP1285922A1 (en) * | 2001-08-13 | 2003-02-26 | Warner-Lambert Company | 1-Alkyl or 1-cycloalkyltriazolo[4,3-a]quinazolin-5-ones as phosphodiesterase inhibitors |
CA2451998A1 (en) | 2001-08-17 | 2003-02-27 | Eli Lilly And Company | Anti-a.beta. antibodies |
US20030195205A1 (en) | 2001-11-02 | 2003-10-16 | Pfizer Inc. | PDE9 inhibitors for treating cardiovascular disorders |
FR2832711B1 (en) | 2001-11-26 | 2004-01-30 | Warner Lambert Co | TRIAZOLO [4,3-A] PYRIDO [2,3-D] PYRIMIDIN-5-ONES DERIVATIVES, COMPOSITIONS CONTAINING SAME, PROCESS FOR PREPARATION AND USE |
PL372887A1 (en) | 2002-02-27 | 2005-08-08 | Pfizer Products Inc. | Acc inhibitors |
DE10238724A1 (en) | 2002-08-23 | 2004-03-04 | Bayer Ag | New 6-alkyl-1,5-dihydro-4H-pyrazolo-(3,4-d)-pyrimidin-4-ones useful as selective phosphodiesterase 9A inhibitors for improving attention, concentration, learning and/or memory performance |
DE10238723A1 (en) | 2002-08-23 | 2004-03-11 | Bayer Ag | Phenyl substituted pyrazolyprimidines |
JP2006519762A (en) | 2002-10-09 | 2006-08-31 | ライナット ニューロサイエンス コーポレイション | Methods for treating Alzheimer's disease using antibodies against amyloid β peptide and compositions thereof |
FR2853329B1 (en) | 2003-04-02 | 2006-07-14 | Onera (Off Nat Aerospatiale) | PROCESS FOR FORMING ON METAL A PROTECTIVE COATING CONTAINING ALUMINUM AND ZIRCONIUM |
US20040220186A1 (en) | 2003-04-30 | 2004-11-04 | Pfizer Inc. | PDE9 inhibitors for treating type 2 diabetes,metabolic syndrome, and cardiovascular disease |
BRPI0410630A (en) | 2003-06-19 | 2006-06-13 | Pfizer Prod Inc | nk1 antagonist |
WO2005025616A1 (en) | 2003-09-09 | 2005-03-24 | Takeda Pharmaceutical Company Limited | Use of antibody |
GB0327319D0 (en) | 2003-11-24 | 2003-12-24 | Pfizer Ltd | Novel pharmaceuticals |
EP1720847A1 (en) | 2004-02-02 | 2006-11-15 | Pfizer Products Incorporated | Histamine-3 receptor modulators |
RU2266906C1 (en) | 2004-04-29 | 2005-12-27 | Общество с ограниченной ответственностью "Исследовательский Институт Химического Разнообразия" (ООО "Исследовательский Институт Химического Разнообразия") | Anellated carbamoyl azaheterocycles, methods for their preparing (variants), pharmaceutical composition, focused library |
ITMI20040874A1 (en) * | 2004-04-30 | 2004-07-30 | Ist Naz Stud Cura Dei Tumori | INDOLIC AND AZAINDOLIC DERIVATIVES WITH ANTI-TUMORAL ACTION |
US7456164B2 (en) | 2004-05-07 | 2008-11-25 | Pfizer, Inc | 3- or 4-monosubtituted phenol and thiophenol derivatives useful as H3 ligands |
EP1595881A1 (en) | 2004-05-12 | 2005-11-16 | Pfizer Limited | Tetrahydronaphthyridine derivates useful as histamine H3 receptor ligands |
GEP20084421B (en) | 2004-05-12 | 2008-07-10 | Pfizer Prod Inc | Proline derivatives and their use as dipeptidyl peptidase iv inhibitors |
EA010888B1 (en) | 2004-05-25 | 2008-12-30 | Пфайзер Продактс, Инк. | Tetraazabenzo[e]azulene derivatives and analogs thereof |
EA016357B1 (en) | 2004-07-30 | 2012-04-30 | Ринат Ньюросайенс Корп. | Antibodies directed against amyloid-beta peptide and methods using same |
GB0423356D0 (en) | 2004-10-21 | 2004-11-24 | Merck Sharp & Dohme | Therapeutic agents |
EP1827493A4 (en) | 2004-12-22 | 2009-09-30 | Univ St Louis | Use of anti-abeta antibody to treat traumatic brain injury |
NZ555491A (en) | 2005-01-03 | 2010-01-29 | Univ Siena | Aryl piperazine derivatives for the treatment of neuropsychiatric disorders |
PA8660701A1 (en) | 2005-02-04 | 2006-09-22 | Pfizer Prod Inc | SMALL AGONISTS AND THEIR USES |
MY148086A (en) | 2005-04-29 | 2013-02-28 | Rinat Neuroscience Corp | Antibodies directed against amyloid-beta peptide and methods using same |
US8227475B2 (en) | 2005-05-12 | 2012-07-24 | Pfizer Inc. | Anhydrous crystalline forms of N-[1-(2-ethoxyethyl)-5-(N-ethyl-N-methylamino)-7-(4-methylpyridin-2-yl-amino)-1H-pyrazolo[4,3-d]pyrimidine-3-carbonyl]methanesulfonamide |
WO2006126082A2 (en) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Pyridine [3,4-b] pyrazinones as pde-5 inhibitors |
WO2006126083A1 (en) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Company Llc | Pyridine [3 , 4-b] pyrazinone compounds as pde-5 inhibitors |
CA2603830A1 (en) | 2005-05-24 | 2006-11-30 | Pharmacia & Upjohn Co Llc | Pyridino [2 , 3-b] pyrazinones as pde-5 inhibitors |
ES2354569T3 (en) | 2005-06-22 | 2011-03-16 | Pfizer Products Inc. | HISTAMINE RECEIVER ANTAGONISTS-3. |
US8158673B2 (en) | 2005-10-27 | 2012-04-17 | Pfizer Inc. | Histamine-3 receptor antagonists |
EP1779849A1 (en) | 2005-10-28 | 2007-05-02 | Nikem Research S.R.L. | V-ATPase inhibitors for the treatment of septic shock |
EP1779848A1 (en) | 2005-10-28 | 2007-05-02 | Nikem Research S.R.L. | V-ATPase inhibitors for the treatment of inflammatory and autoimmune diseases |
JP2009514846A (en) | 2005-11-04 | 2009-04-09 | ファイザー・リミテッド | Tetrahydronaphthyridine derivatives |
WO2007063385A2 (en) | 2005-12-01 | 2007-06-07 | Pfizer Products Inc. | Spirocyclic amine histamine-3 receptor antagonists |
WO2007069053A1 (en) | 2005-12-14 | 2007-06-21 | Pfizer Products Inc. | Benzimidazole antagonists of the h-3 receptor |
WO2007088450A2 (en) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Chromane antagonist of the h-3 receptor |
WO2007088462A1 (en) | 2006-02-01 | 2007-08-09 | Pfizer Products Inc. | Spirochromane antagonists of the h-3 receptor |
WO2007099423A1 (en) | 2006-03-02 | 2007-09-07 | Pfizer Products Inc. | 1-pyrrolidine indane derivatives as histamine-3 receptor antagonists |
CA2643055A1 (en) | 2006-03-13 | 2007-09-20 | Pfizer Products Inc. | Tetralines antagonists of the h-3 receptor |
EP2010520B1 (en) | 2006-04-20 | 2012-09-12 | Pfizer Products Inc. | Heterobicyclic amides for the prevention and treatment of glucokinase-mediated diseases |
WO2007122466A1 (en) | 2006-04-21 | 2007-11-01 | Pfizer Products Inc. | Pyridine[3,4-b]pyrazinones |
WO2007138431A2 (en) | 2006-05-30 | 2007-12-06 | Pfizer Products Inc. | Azabicyclic ether histamine-3 antagonists |
WO2008065508A1 (en) | 2006-11-29 | 2008-06-05 | Pfizer Products Inc. | Spiroketone acetyl-coa carboxylase inhibitors |
CA2676456C (en) | 2007-01-22 | 2012-03-27 | Pfizer Products Inc. | Tosylate salt of a therapeutic compound and pharmaceutical compositions thereof |
US20090036425A1 (en) | 2007-08-02 | 2009-02-05 | Pfizer Inc | Substituted bicyclolactam compounds |
JP5406215B2 (en) | 2008-01-25 | 2014-02-05 | ハイ ポイント ファーマシューティカルズ,リミティド ライアビリティ カンパニー | Tricyclic compounds as regulators of TNF-α synthesis and PDE4 inhibitors |
US20100137320A1 (en) | 2008-02-29 | 2010-06-03 | Schering Corporation | Gamma secretase modulators |
ES2545231T3 (en) | 2008-05-28 | 2015-09-09 | Pfizer Inc. | Pyrazoloespirocetone acetyl-CoA carboxylase inhibitors |
EP2297164A1 (en) | 2008-05-28 | 2011-03-23 | Pfizer Inc. | Pyrazolospiroketone acetyl-coa carboxylase inhibitors |
US20110130365A1 (en) | 2008-07-29 | 2011-06-02 | Benbow John W | Fluorinated Heteroaryls |
PT2334687E (en) | 2008-08-28 | 2012-04-13 | Pfizer | Dioxa-bicyclo[3.2.1.]octane-2,3,4-triol derivatives |
WO2010086820A1 (en) | 2009-02-02 | 2010-08-05 | Pfizer Inc. | 4-amino-5-oxo-7, 8-dihydropyrimido [5,4-f] [1,4] oxazepin-6 (5h) -yl) phenyl derivatives, pharmaceutical compositions and uses thereof |
CN102388038B (en) | 2009-03-11 | 2014-04-23 | 辉瑞大药厂 | Benzofuranyl derivatives used as glucokinase inhibitors |
EP2406230A1 (en) | 2009-03-11 | 2012-01-18 | Pfizer Inc. | Substituted indazole amides and their use as glucokinase activators |
CA2754523A1 (en) | 2009-03-20 | 2010-09-23 | Pfizer Inc. | 3-oxa-7-azabicyclo[3.3.1]nonanes |
WO2010128414A1 (en) | 2009-05-08 | 2010-11-11 | Pfizer Inc. | Gpr 119 modulators |
EP2427450A1 (en) | 2009-05-08 | 2012-03-14 | Pfizer Inc. | Gpr 119 modulators |
MX2011013034A (en) | 2009-06-05 | 2012-02-08 | Pfizer | L- ( piperidin-4-yl) -pyrazole derivatives as gpr 119 modulators. |
WO2011005611A1 (en) | 2009-07-09 | 2011-01-13 | Merck Sharp & Dohme Corp. | Neuromedin u receptor agonists and uses thereof |
EP2831080B1 (en) | 2012-03-29 | 2017-03-15 | Francis Xavier Tavares | Lactam kinase inhibitors |
EP2841417A1 (en) * | 2012-04-26 | 2015-03-04 | Francis Xavier Tavares | Synthesis of lactams |
BR112015019276A2 (en) | 2013-02-19 | 2017-07-18 | Pfizer | azabenzimidazole compounds as inhibitors of pde4 isoenzymes for the treatment of snc disorders and other disorders |
HUE046653T2 (en) | 2013-03-15 | 2020-03-30 | G1 Therapeutics Inc | Transient protection of normal cells during chemotherapy |
EP3119347B1 (en) | 2014-03-21 | 2023-06-07 | Align Technology, Inc. | Segmented orthodontic appliance with elastics |
HUE051898T2 (en) * | 2015-06-17 | 2021-03-29 | Pfizer | Tricyclic compounds and their use as phosphodiesterase inhibitors. |
US10323042B2 (en) * | 2016-02-23 | 2019-06-18 | Pfizer Inc. | 6,7-dihydro-5H-pyrazolo[5,1-b][1,3]oxazine-2-carboxamide compounds |
-
2016
- 2016-06-09 HU HUE16739563A patent/HUE051898T2/en unknown
- 2016-06-09 ES ES16739563T patent/ES2832893T3/en active Active
- 2016-06-09 JP JP2017564677A patent/JP6827959B2/en active Active
- 2016-06-09 CN CN201680034997.XA patent/CN107787322B/en active Active
- 2016-06-09 PL PL16739563T patent/PL3310784T3/en unknown
- 2016-06-09 EP EP20193125.0A patent/EP3766885B1/en active Active
- 2016-06-09 ES ES20193125T patent/ES2924371T3/en active Active
- 2016-06-09 DK DK20193125.0T patent/DK3766885T3/en active
- 2016-06-09 PT PT167395631T patent/PT3310784T/en unknown
- 2016-06-09 CA CA2989456A patent/CA2989456C/en active Active
- 2016-06-09 SG SG10201912333PA patent/SG10201912333PA/en unknown
- 2016-06-09 EP EP16739563.1A patent/EP3310784B1/en active Active
- 2016-06-09 WO PCT/IB2016/053398 patent/WO2016203347A1/en active Application Filing
- 2016-06-09 AU AU2016280137A patent/AU2016280137B2/en active Active
- 2016-06-09 EA EA201792425A patent/EA039714B1/en unknown
- 2016-06-09 TN TNP/2017/000485A patent/TN2017000485A1/en unknown
- 2016-06-09 CU CUP2017000153A patent/CU20170153A7/en unknown
- 2016-06-09 BR BR112017026191-0A patent/BR112017026191B1/en active IP Right Grant
- 2016-06-09 KR KR1020207014430A patent/KR102426986B1/en active IP Right Grant
- 2016-06-09 HU HUE20193125A patent/HUE059372T2/en unknown
- 2016-06-09 DK DK16739563.1T patent/DK3310784T3/en active
- 2016-06-09 MX MX2017016149A patent/MX2017016149A/en unknown
- 2016-06-09 PL PL20193125.0T patent/PL3766885T3/en unknown
- 2016-06-09 US US15/736,942 patent/US11472805B2/en active Active
- 2016-06-09 PT PT201931250T patent/PT3766885T/en unknown
- 2016-06-09 CR CR20170572A patent/CR20170572A/en unknown
- 2016-06-09 KR KR1020177036051A patent/KR20180004817A/en active Application Filing
- 2016-06-09 UA UAA201710872A patent/UA125334C2/en unknown
- 2016-06-09 PE PE2017002730A patent/PE20180478A1/en not_active Application Discontinuation
- 2016-06-14 TW TW105118595A patent/TWI623538B/en active
-
2017
- 2017-11-05 IL IL255444A patent/IL255444B/en active IP Right Grant
- 2017-12-11 PH PH12017502260A patent/PH12017502260A1/en unknown
- 2017-12-14 DO DO2017000297A patent/DOP2017000297A/en unknown
- 2017-12-19 CO CONC2017/0012994A patent/CO2017012994A2/en unknown
-
2018
- 2018-01-16 EC ECIEPI20183372A patent/ECSP18003372A/en unknown
- 2018-04-25 HK HK18105387.0A patent/HK1245790A1/en unknown
- 2018-10-24 HK HK18113640.7A patent/HK1254661A1/en unknown
-
2021
- 2021-01-15 AU AU2021200232A patent/AU2021200232A1/en not_active Abandoned
-
2022
- 2022-08-12 US US17/886,807 patent/US20230002386A1/en active Pending
- 2022-10-12 US US17/964,491 patent/US20230146535A1/en active Pending
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
IL247949A0 (en) | Novel pyrazolo pyrimidine derivatives and their use as malt1 inhibitors | |
IL251932B (en) | Benzylpropargylether as nitrification inhibitors | |
IL264258B (en) | Substituted diazahetero-bicyclic compounds and their use | |
SG11201708027XA (en) | Compounds and their use as bace1 inhibitors | |
HK1244486A1 (en) | Tricyclic dlk inhibitors and uses thereof | |
IL251778B (en) | New pyrazolopyrimidine derivatives as nik inhibitors | |
HK1258849A1 (en) | Tricyclic pi3k inhibitor compounds and methods of use | |
HK1254661A1 (en) | Tricyclic compounds and their use as phosphodiesterase inhibitors | |
HK1231468A1 (en) | Tricyclic compound and jak inhibitor jak | |
HK1250161B (en) | 6-morpholinyl-2-pyrazolyl-9h-purine derivatives and their use as pi3k inhibitors | |
HK1250028A1 (en) | 2-phenyl-6-imidazolyl-pyridine-4-carboxamide derivatives and their use as eaat3 inhibitors | |
PL3268356T3 (en) | Heterocyclic compounds and methods for their use | |
GB201609580D0 (en) | Novel compounds and their use as kinase inhibitors | |
GB201705201D0 (en) | Novel compounds and their use as kinase inhibitors | |
GB201509381D0 (en) | Novel compounds and their use as kinase inhibitors | |
GB201505460D0 (en) | Novel compounds and their use as kinase inhibitors | |
GB201409661D0 (en) | Novel compounds and their use as kinase inhibitors | |
GB201405532D0 (en) | Novel compounds and their use as Kinase inhibitors | |
GB201514770D0 (en) | Compounds and their use | |
GB201513318D0 (en) | Novel compounds and their use |